Incidental Mutation 'R5896:Magi1'
ID |
457512 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Magi1
|
Ensembl Gene |
ENSMUSG00000045095 |
Gene Name |
membrane associated guanylate kinase, WW and PDZ domain containing 1 |
Synonyms |
Baiap1, Gukmi1, AIP3, BAP1, WWP3 |
MMRRC Submission |
044095-MU
|
Accession Numbers |
|
Essential gene? |
Possibly essential
(E-score: 0.561)
|
Stock # |
R5896 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
6 |
Chromosomal Location |
93652436-94260898 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to A
at 93685180 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Serine to Cysteine
at position 506
(S506C)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000145515
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000055224]
[ENSMUST00000089317]
[ENSMUST00000093769]
[ENSMUST00000203519]
[ENSMUST00000203688]
[ENSMUST00000204347]
[ENSMUST00000204532]
|
AlphaFold |
Q6RHR9 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000055224
AA Change: S720C
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000062085 Gene: ENSMUSG00000045095 AA Change: S720C
Domain | Start | End | E-Value | Type |
PDZ
|
26 |
105 |
8.04e-5 |
SMART |
GuKc
|
111 |
295 |
2.55e-49 |
SMART |
WW
|
301 |
333 |
9.65e-11 |
SMART |
WW
|
348 |
380 |
2.88e-9 |
SMART |
low complexity region
|
390 |
402 |
N/A |
INTRINSIC |
low complexity region
|
410 |
428 |
N/A |
INTRINSIC |
PDZ
|
460 |
536 |
3.71e-18 |
SMART |
PDZ
|
631 |
703 |
4.68e-15 |
SMART |
low complexity region
|
707 |
714 |
N/A |
INTRINSIC |
low complexity region
|
720 |
733 |
N/A |
INTRINSIC |
PDZ
|
800 |
876 |
4.64e-19 |
SMART |
low complexity region
|
920 |
942 |
N/A |
INTRINSIC |
PDB:1UEW|A
|
945 |
977 |
2e-6 |
PDB |
PDZ
|
1043 |
1117 |
1.26e-20 |
SMART |
low complexity region
|
1152 |
1164 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000089317
AA Change: S733C
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000086730 Gene: ENSMUSG00000045095 AA Change: S733C
Domain | Start | End | E-Value | Type |
PDZ
|
26 |
105 |
4e-7 |
SMART |
GuKc
|
111 |
295 |
1.3e-51 |
SMART |
WW
|
301 |
333 |
5.8e-13 |
SMART |
WW
|
360 |
392 |
1.7e-11 |
SMART |
low complexity region
|
402 |
414 |
N/A |
INTRINSIC |
low complexity region
|
422 |
440 |
N/A |
INTRINSIC |
PDZ
|
472 |
548 |
1.9e-20 |
SMART |
PDZ
|
643 |
715 |
2.3e-17 |
SMART |
low complexity region
|
733 |
746 |
N/A |
INTRINSIC |
PDZ
|
841 |
917 |
2.4e-21 |
SMART |
low complexity region
|
961 |
983 |
N/A |
INTRINSIC |
PDZ
|
999 |
1074 |
6.1e-25 |
SMART |
PDZ
|
1140 |
1214 |
6.1e-23 |
SMART |
low complexity region
|
1347 |
1357 |
N/A |
INTRINSIC |
low complexity region
|
1366 |
1423 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000093769
AA Change: S505C
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000091283 Gene: ENSMUSG00000045095 AA Change: S505C
Domain | Start | End | E-Value | Type |
low complexity region
|
10 |
15 |
N/A |
INTRINSIC |
WW
|
74 |
106 |
9.65e-11 |
SMART |
WW
|
133 |
165 |
2.88e-9 |
SMART |
low complexity region
|
175 |
187 |
N/A |
INTRINSIC |
low complexity region
|
195 |
213 |
N/A |
INTRINSIC |
PDZ
|
245 |
321 |
3.71e-18 |
SMART |
PDZ
|
416 |
488 |
4.68e-15 |
SMART |
low complexity region
|
492 |
499 |
N/A |
INTRINSIC |
low complexity region
|
505 |
518 |
N/A |
INTRINSIC |
PDZ
|
613 |
689 |
4.64e-19 |
SMART |
low complexity region
|
733 |
755 |
N/A |
INTRINSIC |
PDZ
|
771 |
858 |
2.3e-23 |
SMART |
PDZ
|
924 |
998 |
1.26e-20 |
SMART |
low complexity region
|
1131 |
1141 |
N/A |
INTRINSIC |
low complexity region
|
1150 |
1207 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000203519
AA Change: S732C
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000145244 Gene: ENSMUSG00000045095 AA Change: S732C
Domain | Start | End | E-Value | Type |
PDZ
|
26 |
105 |
8.04e-5 |
SMART |
GuKc
|
111 |
295 |
2.55e-49 |
SMART |
WW
|
301 |
333 |
9.65e-11 |
SMART |
WW
|
360 |
392 |
2.88e-9 |
SMART |
low complexity region
|
402 |
414 |
N/A |
INTRINSIC |
low complexity region
|
422 |
440 |
N/A |
INTRINSIC |
PDZ
|
472 |
548 |
3.71e-18 |
SMART |
PDZ
|
643 |
715 |
4.68e-15 |
SMART |
low complexity region
|
719 |
726 |
N/A |
INTRINSIC |
low complexity region
|
732 |
745 |
N/A |
INTRINSIC |
PDZ
|
812 |
888 |
4.64e-19 |
SMART |
low complexity region
|
932 |
954 |
N/A |
INTRINSIC |
PDB:1UEW|A
|
957 |
989 |
2e-6 |
PDB |
PDZ
|
1055 |
1115 |
1.13e-8 |
SMART |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000203688
AA Change: S506C
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000145515 Gene: ENSMUSG00000045095 AA Change: S506C
Domain | Start | End | E-Value | Type |
Pfam:MAGI_u1
|
1 |
34 |
2.9e-17 |
PFAM |
WW
|
74 |
106 |
9.65e-11 |
SMART |
WW
|
133 |
165 |
2.88e-9 |
SMART |
low complexity region
|
175 |
187 |
N/A |
INTRINSIC |
low complexity region
|
195 |
213 |
N/A |
INTRINSIC |
PDZ
|
245 |
321 |
3.71e-18 |
SMART |
PDZ
|
416 |
488 |
4.68e-15 |
SMART |
low complexity region
|
506 |
519 |
N/A |
INTRINSIC |
PDZ
|
614 |
690 |
4.64e-19 |
SMART |
low complexity region
|
734 |
756 |
N/A |
INTRINSIC |
PDZ
|
772 |
858 |
1.74e-23 |
SMART |
PDZ
|
924 |
998 |
1.26e-20 |
SMART |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000204347
AA Change: S733C
PolyPhen 2
Score 0.652 (Sensitivity: 0.87; Specificity: 0.91)
|
SMART Domains |
Protein: ENSMUSP00000144881 Gene: ENSMUSG00000045095 AA Change: S733C
Domain | Start | End | E-Value | Type |
PDZ
|
26 |
105 |
4e-7 |
SMART |
GuKc
|
111 |
295 |
1.3e-51 |
SMART |
WW
|
301 |
333 |
5.8e-13 |
SMART |
WW
|
360 |
392 |
1.7e-11 |
SMART |
low complexity region
|
402 |
414 |
N/A |
INTRINSIC |
low complexity region
|
422 |
440 |
N/A |
INTRINSIC |
PDZ
|
472 |
548 |
1.9e-20 |
SMART |
PDZ
|
643 |
715 |
2.3e-17 |
SMART |
low complexity region
|
733 |
746 |
N/A |
INTRINSIC |
PDZ
|
841 |
917 |
2.4e-21 |
SMART |
low complexity region
|
961 |
983 |
N/A |
INTRINSIC |
PDZ
|
999 |
1086 |
1.1e-25 |
SMART |
PDZ
|
1152 |
1226 |
6.1e-23 |
SMART |
low complexity region
|
1261 |
1273 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000204532
AA Change: Q494L
PolyPhen 2
Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
|
SMART Domains |
Protein: ENSMUSP00000144769 Gene: ENSMUSG00000045095 AA Change: Q494L
Domain | Start | End | E-Value | Type |
Pfam:MAGI_u1
|
1 |
34 |
1.8e-14 |
PFAM |
WW
|
74 |
106 |
5.8e-13 |
SMART |
WW
|
133 |
165 |
1.7e-11 |
SMART |
low complexity region
|
175 |
187 |
N/A |
INTRINSIC |
low complexity region
|
195 |
213 |
N/A |
INTRINSIC |
PDZ
|
245 |
321 |
1.9e-20 |
SMART |
PDZ
|
416 |
488 |
7.3e-17 |
SMART |
|
Coding Region Coverage |
- 1x: 99.9%
- 3x: 99.5%
- 10x: 97.3%
- 20x: 91.5%
|
Validation Efficiency |
99% (86/87) |
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene is a member of the membrane-associated guanylate kinase homologue (MAGUK) family. MAGUK proteins participate in the assembly of multiprotein complexes on the inner surface of the plasma membrane at regions of cell-cell contact. The product of this gene may play a role as scaffolding protein at cell-cell junctions. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]
|
Allele List at MGI |
All alleles(165) : Targeted(2) Gene trapped(163)
|
Other mutations in this stock |
Total: 75 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310061N02Rik |
A |
T |
16: 88,504,321 (GRCm39) |
S159T |
probably damaging |
Het |
2610028H24Rik |
T |
A |
10: 76,288,664 (GRCm39) |
M53K |
probably benign |
Het |
3425401B19Rik |
G |
A |
14: 32,383,632 (GRCm39) |
Q778* |
probably null |
Het |
Abhd16a |
T |
A |
17: 35,310,701 (GRCm39) |
|
probably benign |
Het |
Acp6 |
A |
G |
3: 97,075,810 (GRCm39) |
K226R |
probably benign |
Het |
Ankfy1 |
A |
G |
11: 72,650,811 (GRCm39) |
D998G |
probably damaging |
Het |
Apbb1 |
G |
T |
7: 105,223,432 (GRCm39) |
P60T |
probably damaging |
Het |
Apol9a |
T |
A |
15: 77,288,705 (GRCm39) |
I221F |
probably benign |
Het |
Arhgap29 |
A |
G |
3: 121,805,736 (GRCm39) |
E947G |
possibly damaging |
Het |
B430218F22Rik |
A |
T |
13: 118,523,934 (GRCm39) |
|
probably benign |
Het |
Carmil3 |
ACCCCC |
ACCCCCCC |
14: 55,741,456 (GRCm39) |
|
probably null |
Het |
Ccdc69 |
C |
T |
11: 54,943,716 (GRCm39) |
|
probably null |
Het |
Ccdc93 |
G |
T |
1: 121,390,849 (GRCm39) |
V274L |
possibly damaging |
Het |
Cdc25a |
A |
G |
9: 109,713,433 (GRCm39) |
D191G |
probably benign |
Het |
Cimip2a |
A |
T |
2: 25,110,578 (GRCm39) |
M129L |
probably benign |
Het |
Cmya5 |
A |
G |
13: 93,182,373 (GRCm39) |
|
probably null |
Het |
Crebzf |
TGGAGGAGGAGGAGGAGGA |
TGGAGGAGGAGGAGGA |
7: 90,092,479 (GRCm39) |
|
probably benign |
Het |
Csde1 |
T |
C |
3: 102,947,859 (GRCm39) |
|
probably benign |
Het |
Ctdp1 |
A |
G |
18: 80,502,003 (GRCm39) |
L177P |
probably damaging |
Het |
Dnah5 |
T |
A |
15: 28,272,206 (GRCm39) |
H1003Q |
probably benign |
Het |
Epb41l2 |
T |
A |
10: 25,369,494 (GRCm39) |
N604K |
probably damaging |
Het |
Fig4 |
T |
A |
10: 41,130,881 (GRCm39) |
N465Y |
possibly damaging |
Het |
Gemin7 |
G |
A |
7: 19,299,223 (GRCm39) |
S124F |
probably damaging |
Het |
Gli3 |
G |
A |
13: 15,900,765 (GRCm39) |
R1384K |
probably benign |
Het |
Gm12258 |
G |
A |
11: 58,750,457 (GRCm39) |
C544Y |
probably damaging |
Het |
Grm1 |
C |
T |
10: 10,956,294 (GRCm39) |
|
probably benign |
Het |
H2-T15 |
T |
A |
17: 36,367,236 (GRCm39) |
M329L |
probably benign |
Het |
Hps4 |
C |
T |
5: 112,517,351 (GRCm39) |
T246I |
probably benign |
Het |
Ifngr2 |
A |
T |
16: 91,358,653 (GRCm39) |
E284D |
possibly damaging |
Het |
Impdh2 |
A |
G |
9: 108,441,165 (GRCm39) |
T148A |
probably benign |
Het |
Irx3 |
T |
C |
8: 92,527,763 (GRCm39) |
S36G |
probably benign |
Het |
Itga5 |
T |
A |
15: 103,259,514 (GRCm39) |
K667N |
probably benign |
Het |
Itgad |
G |
A |
7: 127,773,188 (GRCm39) |
C15Y |
probably benign |
Het |
Ly75 |
T |
G |
2: 60,213,490 (GRCm39) |
E29A |
probably benign |
Het |
Map4 |
G |
A |
9: 109,901,702 (GRCm39) |
V781M |
possibly damaging |
Het |
Med23 |
T |
C |
10: 24,778,043 (GRCm39) |
L797P |
probably damaging |
Het |
Naip1 |
C |
T |
13: 100,559,636 (GRCm39) |
G1123R |
probably benign |
Het |
Ncor1 |
G |
T |
11: 62,274,016 (GRCm39) |
P55Q |
probably damaging |
Het |
Odr4 |
A |
T |
1: 150,256,111 (GRCm39) |
N211K |
probably benign |
Het |
Ofcc1 |
T |
A |
13: 40,334,060 (GRCm39) |
I344F |
probably benign |
Het |
Or4a74 |
C |
A |
2: 89,439,667 (GRCm39) |
V260F |
probably damaging |
Het |
Or4d5 |
A |
T |
9: 40,012,189 (GRCm39) |
M199K |
probably damaging |
Het |
Or5d35 |
A |
G |
2: 87,855,465 (GRCm39) |
Y133C |
probably damaging |
Het |
Or5k1 |
G |
A |
16: 58,618,095 (GRCm39) |
T38I |
probably damaging |
Het |
Otub2 |
C |
T |
12: 103,369,687 (GRCm39) |
|
probably benign |
Het |
Parva |
A |
G |
7: 112,143,960 (GRCm39) |
M83V |
probably benign |
Het |
Pcdha8 |
T |
A |
18: 37,126,572 (GRCm39) |
N351K |
probably benign |
Het |
Pcdhb5 |
T |
A |
18: 37,455,732 (GRCm39) |
L704* |
probably null |
Het |
Pkd1l3 |
T |
A |
8: 110,353,468 (GRCm39) |
L683H |
probably damaging |
Het |
Plekhn1 |
C |
T |
4: 156,308,331 (GRCm39) |
R288H |
probably benign |
Het |
Polr2a |
A |
T |
11: 69,627,086 (GRCm39) |
N1457K |
probably damaging |
Het |
Ppp1r12b |
A |
G |
1: 134,693,719 (GRCm39) |
S981P |
probably damaging |
Het |
Ppp1r9a |
A |
G |
6: 5,159,648 (GRCm39) |
K1062E |
probably damaging |
Het |
Ptpre |
A |
T |
7: 135,276,007 (GRCm39) |
T498S |
probably benign |
Het |
Pus7l |
C |
T |
15: 94,427,332 (GRCm39) |
|
probably null |
Het |
Rptn |
C |
T |
3: 93,305,639 (GRCm39) |
Q991* |
probably null |
Het |
Rsu1 |
T |
G |
2: 13,229,170 (GRCm39) |
E76A |
probably damaging |
Het |
Septin11 |
T |
A |
5: 93,304,824 (GRCm39) |
F214I |
probably damaging |
Het |
Slc1a7 |
G |
T |
4: 107,869,587 (GRCm39) |
A551S |
probably benign |
Het |
Slc45a2 |
T |
A |
15: 11,000,941 (GRCm39) |
Y13* |
probably null |
Het |
Slc7a14 |
T |
G |
3: 31,311,719 (GRCm39) |
L100F |
probably damaging |
Het |
Slit3 |
A |
G |
11: 35,598,932 (GRCm39) |
E1512G |
probably damaging |
Het |
Stat5a |
A |
G |
11: 100,767,883 (GRCm39) |
Q458R |
possibly damaging |
Het |
Svep1 |
T |
C |
4: 58,084,906 (GRCm39) |
T1811A |
possibly damaging |
Het |
Tarbp1 |
A |
G |
8: 127,179,667 (GRCm39) |
F624L |
probably benign |
Het |
Tfeb |
T |
G |
17: 48,070,433 (GRCm39) |
|
probably null |
Het |
Tnxb |
G |
A |
17: 34,891,126 (GRCm39) |
G490R |
probably damaging |
Het |
Tra2b |
T |
C |
16: 22,077,953 (GRCm39) |
Y32C |
probably damaging |
Het |
Trpv4 |
C |
T |
5: 114,760,708 (GRCm39) |
|
probably benign |
Het |
Uvrag |
A |
T |
7: 98,637,414 (GRCm39) |
L138* |
probably null |
Het |
Vwf |
A |
T |
6: 125,655,725 (GRCm39) |
|
probably null |
Het |
Wdr47 |
G |
A |
3: 108,526,322 (GRCm39) |
D282N |
probably damaging |
Het |
Xirp2 |
A |
G |
2: 67,340,290 (GRCm39) |
N844D |
possibly damaging |
Het |
Xirp2 |
A |
G |
2: 67,339,042 (GRCm39) |
M428V |
probably benign |
Het |
Znfx1 |
G |
A |
2: 166,880,920 (GRCm39) |
T288I |
probably damaging |
Het |
|
Other mutations in Magi1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01376:Magi1
|
APN |
6 |
94,260,074 (GRCm39) |
missense |
possibly damaging |
0.86 |
IGL01457:Magi1
|
APN |
6 |
93,724,205 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01642:Magi1
|
APN |
6 |
93,663,605 (GRCm39) |
missense |
possibly damaging |
0.69 |
IGL01724:Magi1
|
APN |
6 |
93,769,381 (GRCm39) |
splice site |
probably null |
|
IGL01967:Magi1
|
APN |
6 |
93,685,115 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01984:Magi1
|
APN |
6 |
93,685,155 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02074:Magi1
|
APN |
6 |
93,722,579 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02098:Magi1
|
APN |
6 |
93,655,768 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02225:Magi1
|
APN |
6 |
93,671,007 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02522:Magi1
|
APN |
6 |
93,655,617 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL02659:Magi1
|
APN |
6 |
93,762,591 (GRCm39) |
missense |
possibly damaging |
0.68 |
IGL02900:Magi1
|
APN |
6 |
93,663,854 (GRCm39) |
missense |
probably damaging |
1.00 |
P0007:Magi1
|
UTSW |
6 |
93,722,969 (GRCm39) |
missense |
probably damaging |
1.00 |
R0149:Magi1
|
UTSW |
6 |
93,724,226 (GRCm39) |
missense |
probably damaging |
1.00 |
R0512:Magi1
|
UTSW |
6 |
93,671,045 (GRCm39) |
missense |
probably damaging |
1.00 |
R1487:Magi1
|
UTSW |
6 |
93,685,060 (GRCm39) |
missense |
probably benign |
0.00 |
R1497:Magi1
|
UTSW |
6 |
93,724,310 (GRCm39) |
missense |
probably damaging |
1.00 |
R1502:Magi1
|
UTSW |
6 |
93,671,151 (GRCm39) |
missense |
probably damaging |
1.00 |
R1824:Magi1
|
UTSW |
6 |
93,676,620 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2042:Magi1
|
UTSW |
6 |
93,732,026 (GRCm39) |
missense |
probably benign |
|
R2132:Magi1
|
UTSW |
6 |
93,674,255 (GRCm39) |
missense |
probably damaging |
0.99 |
R2331:Magi1
|
UTSW |
6 |
93,662,543 (GRCm39) |
missense |
probably damaging |
1.00 |
R2418:Magi1
|
UTSW |
6 |
93,722,891 (GRCm39) |
missense |
probably damaging |
1.00 |
R3076:Magi1
|
UTSW |
6 |
93,734,668 (GRCm39) |
missense |
possibly damaging |
0.63 |
R3551:Magi1
|
UTSW |
6 |
93,676,610 (GRCm39) |
missense |
probably damaging |
0.98 |
R4005:Magi1
|
UTSW |
6 |
93,678,299 (GRCm39) |
missense |
probably damaging |
1.00 |
R4455:Magi1
|
UTSW |
6 |
93,762,438 (GRCm39) |
missense |
probably damaging |
1.00 |
R4670:Magi1
|
UTSW |
6 |
93,663,624 (GRCm39) |
splice site |
probably null |
|
R4671:Magi1
|
UTSW |
6 |
93,657,768 (GRCm39) |
critical splice donor site |
probably null |
|
R4839:Magi1
|
UTSW |
6 |
93,671,177 (GRCm39) |
missense |
probably damaging |
1.00 |
R5132:Magi1
|
UTSW |
6 |
93,660,072 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5147:Magi1
|
UTSW |
6 |
93,724,248 (GRCm39) |
missense |
probably damaging |
1.00 |
R5525:Magi1
|
UTSW |
6 |
93,769,354 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5724:Magi1
|
UTSW |
6 |
93,722,682 (GRCm39) |
missense |
probably damaging |
1.00 |
R5724:Magi1
|
UTSW |
6 |
93,657,852 (GRCm39) |
missense |
probably benign |
0.03 |
R5846:Magi1
|
UTSW |
6 |
93,662,584 (GRCm39) |
missense |
probably damaging |
1.00 |
R5912:Magi1
|
UTSW |
6 |
93,685,126 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6112:Magi1
|
UTSW |
6 |
93,722,571 (GRCm39) |
missense |
probably damaging |
1.00 |
R6115:Magi1
|
UTSW |
6 |
93,685,051 (GRCm39) |
missense |
possibly damaging |
0.64 |
R6351:Magi1
|
UTSW |
6 |
93,920,210 (GRCm39) |
missense |
possibly damaging |
0.82 |
R6355:Magi1
|
UTSW |
6 |
94,260,177 (GRCm39) |
missense |
probably benign |
0.06 |
R6457:Magi1
|
UTSW |
6 |
93,676,620 (GRCm39) |
missense |
probably damaging |
1.00 |
R6464:Magi1
|
UTSW |
6 |
93,676,770 (GRCm39) |
missense |
probably damaging |
1.00 |
R6613:Magi1
|
UTSW |
6 |
93,722,654 (GRCm39) |
missense |
probably damaging |
1.00 |
R6661:Magi1
|
UTSW |
6 |
93,920,289 (GRCm39) |
missense |
probably benign |
0.08 |
R6755:Magi1
|
UTSW |
6 |
93,685,158 (GRCm39) |
missense |
probably damaging |
1.00 |
R6909:Magi1
|
UTSW |
6 |
93,674,301 (GRCm39) |
missense |
probably damaging |
1.00 |
R7180:Magi1
|
UTSW |
6 |
93,792,731 (GRCm39) |
missense |
probably benign |
0.10 |
R7224:Magi1
|
UTSW |
6 |
93,660,070 (GRCm39) |
missense |
probably benign |
0.34 |
R7447:Magi1
|
UTSW |
6 |
93,722,562 (GRCm39) |
missense |
possibly damaging |
0.63 |
R7517:Magi1
|
UTSW |
6 |
93,685,189 (GRCm39) |
missense |
probably damaging |
0.99 |
R7537:Magi1
|
UTSW |
6 |
93,685,091 (GRCm39) |
nonsense |
probably null |
|
R7549:Magi1
|
UTSW |
6 |
93,685,095 (GRCm39) |
missense |
probably benign |
0.19 |
R7566:Magi1
|
UTSW |
6 |
93,655,308 (GRCm39) |
missense |
probably benign |
0.03 |
R7805:Magi1
|
UTSW |
6 |
93,659,927 (GRCm39) |
missense |
probably benign |
|
R8022:Magi1
|
UTSW |
6 |
93,674,346 (GRCm39) |
missense |
probably damaging |
1.00 |
R8290:Magi1
|
UTSW |
6 |
94,260,066 (GRCm39) |
missense |
probably damaging |
1.00 |
R8519:Magi1
|
UTSW |
6 |
93,681,330 (GRCm39) |
missense |
possibly damaging |
0.83 |
R8762:Magi1
|
UTSW |
6 |
93,792,789 (GRCm39) |
nonsense |
probably null |
|
R8894:Magi1
|
UTSW |
6 |
93,663,586 (GRCm39) |
missense |
probably benign |
0.12 |
R8974:Magi1
|
UTSW |
6 |
93,674,223 (GRCm39) |
missense |
probably damaging |
1.00 |
R9225:Magi1
|
UTSW |
6 |
93,762,511 (GRCm39) |
missense |
possibly damaging |
0.64 |
R9277:Magi1
|
UTSW |
6 |
93,920,234 (GRCm39) |
missense |
possibly damaging |
0.48 |
R9300:Magi1
|
UTSW |
6 |
93,724,209 (GRCm39) |
missense |
probably damaging |
1.00 |
R9393:Magi1
|
UTSW |
6 |
93,659,890 (GRCm39) |
missense |
probably benign |
0.27 |
R9402:Magi1
|
UTSW |
6 |
94,260,278 (GRCm39) |
missense |
probably benign |
0.00 |
R9432:Magi1
|
UTSW |
6 |
93,660,058 (GRCm39) |
missense |
probably damaging |
1.00 |
R9567:Magi1
|
UTSW |
6 |
93,659,931 (GRCm39) |
critical splice donor site |
probably null |
|
R9567:Magi1
|
UTSW |
6 |
93,655,431 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Predicted Primers |
PCR Primer
(F):5'- TGGGCCCAGATTTTAAAAGGATC -3'
(R):5'- AGAGAACACCATGCTCTGTGG -3'
Sequencing Primer
(F):5'- AAAAGGATCTGGCTTTTTCTGC -3'
(R):5'- GAGGATTTATCTGCATCCAACAC -3'
|
Posted On |
2017-02-15 |